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Compound Detail

CHEMBL165935

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O=C1c2c(O)cccc2C(C(=O)Cc2ccc(Cl)cc2)c2cccc(O)c21
ChEMBL ↗ Properties Compare Identifier

Basic Information

ChEMBL ID CHEMBL165935
Phase Preclinical
Structure Type MOL
InChI Key SSOKSAQOTXVRAL-UHFFFAOYSA-N
2
Targets
2
Activities
1
Assay Types
0
PK Parameters
3
Publications
0
Known Names

Molecular Properties

378.8
MW (Da)
4.24
ALogP
4
HBA
2
HBD
74.6
PSA (Ų)
0.71
QED
0
Ro5 Violations
3
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C22H15ClO4
MW 378.81
Aromatic Rings 3
Heavy Atoms 27
NP-Likeness 0.18

Activity Summary

IC50 2 meas. best 6.0

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Unchecked
CHEMBL612545
 IC50 6.0 6.0 1000.0 1
ADMET
CHEMBL612558
 IC50 5.66 5.66 2200.0 1

Activity Data Samples

Top measurements by pChEMBL value

Target Type Rel. Value Units pChEMBL Assay PubMed
Unchecked IC50 = 1000.0 nM 6.0 Inhibition of LTB4 biosynthesis in bovine polymorphonuclear leukocytes using nor... 11262091
ADMET IC50 = 2200.0 nM 5.66 Concentration required to inhibit 50% growth of HaCaT cells 11262091

Literature References

PubMed DOI Target Context # Activities
11262091 10.1021/jm001073w Unchecked 2
11262091 10.1021/jm001073w ADMET 1
11262091 10.1021/jm001073w No relevant target 1

Data from ChEMBL 36 via Core Engine